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Serum HIV RNA levels were determined by quantitative PCR.
Using these DNA samples, the concentration of proviral DNA was determined by quantitative PCR.
The content of the specified constituent must be determined by quantitative analysis.
e, Gene expression levels of IFNG, IL17A, IL4, CXCR3 and CCR6, determined by quantitative PCR (normalized to RPL13A).
The concentration of proinflammatory cytokines and chemokines in CVL was determined by quantitative ELISA.
Abundance of mRNA for PCC, PC, and PEPCK was determined by quantitative reverse-transcription PCR.
It also resulted in significant tissue preservation as determined by quantitative histomorphometry.
METHODS: The expression of pro-angiogenic genes was determined by quantitative real-time RT-PCR.
The transfection efficiency was determined by quantitative RT-PCR for hsa-miR-10a.
Transcription level of seven sites within rDNA unit was determined by quantitative real-time PCR.
rDNA copy number in ∆fob1Sup mutants with or without pRRN5 determined by quantitative real-time PCR.
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